DisGeNET - a database of gene-disease associations

Heart failure, C0018801

Variant: rs397516089 ×

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs397516089

rs397516089

MYH7

0.010

GeneticVariation

BEFREE

A second pediatric patient presented with heart failure and was found to carry a de novo MYH7 R369Q mutation.

2009